|
NM_014844.5:c.2394+3A>G
MANE Select
|
NP_055659.2:n.2394+3A>G
|
|
ENST00000359520.12:c.2394+3A>G
MANE Select
|
ENSP00000352510.7:n.2394+3A>G
|
|
NM_001172631.1:c.2394+3A>G
|
NP_001166102.1:n.2394+3A>G
|
|
NM_001172631.2:c.2394+3A>G
|
NP_001166102.1:n.2394+3A>G
|
|
NM_001172631.3:c.2394+3A>G
|
NP_001166102.1:n.2394+3A>G
|
|
NM_014844.3:c.2394+3A>G
|
NP_055659.2:n.2394+3A>G
|
|
NM_014844.4:c.2394+3A>G
|
NP_055659.2:n.2394+3A>G
|
|
ENST00000359520.11:c.2394+3A>G
|
ENSP00000352510.7:n.2394+3A>G
|
|
ENST00000558678.1:c.2394+3A>G
|
ENSP00000453671.1:n.2394+3A>G
|
|
ENST00000560060.5:n.190+3A>G
|
|
|
XM_005268246.2:c.2061+3A>G
|
XP_005268303.1:n.2061+3A>G
|
|
XM_011537419.1:c.2394+3A>G
|
XP_011535721.1:n.2394+3A>G
|